Class ITerminated in FDA datasetRecall initiated Apr 5, 2023

Revolution Farms Robust Romaine plastic 5oz Retail container

Recalling firm: Caledonia Facility of Revolution Farms LLC

Why it was recalled

Listeria monocytogenes

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 9, 2023.

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ProductRevolution Farms Robust Romaine plastic 5oz Retail container UPC 856791008035 and 3lb bulk clear poly bag UPC 856791008127 Revolution Farms Romaine Lettuce Boats plastic 5oz Retail container UPC 856791008196 Revolution Farms Whole Leaf Romaine plastic 5oz Retail container UPC 856791008202
Package size5oz
UPC856791008035, 856791008127, 856791008196, 856791008202

FDA code information

Best By 3/28/23 - 4/5/23

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Full FDA record and distribution details

Original product description

Revolution Farms Robust Romaine plastic 5oz Retail container UPC 856791008035 and 3lb bulk clear poly bag UPC 856791008127 Revolution Farms Romaine Lettuce Boats plastic 5oz Retail container UPC 856791008196 Revolution Farms Whole Leaf Romaine plastic 5oz Retail container UPC 856791008202

Extracted codes and context

TypeCode / valueContext
UPC856791008035Revolution Farms Robust Romaine plastic 5oz Retail container UPC 856791008035 and 3lb bulk clear poly bag UPC 856791008127 Revolution Farms Romaine Lettuce Boats plastic 5oz Retail container UPC
UPC856791008127 plastic 5oz Retail container UPC 856791008035 and 3lb bulk clear poly bag UPC 856791008127 Revolution Farms Romaine Lettuce Boats plastic 5oz Retail container UPC 856791008196 Revolution Farms Whole Leaf Roma
UPC85679100819608127 Revolution Farms Romaine Lettuce Boats plastic 5oz Retail container UPC 856791008196 Revolution Farms Whole Leaf Romaine plastic 5oz Retail container UPC 856791008202
UPC856791008202791008196 Revolution Farms Whole Leaf Romaine plastic 5oz Retail container UPC 856791008202

Original FDA recall reason

Listeria monocytogenes

Recall details

Recall number
F-0824-2023
Event ID
92065
FDA status
Terminated
Initiated
Apr 5, 2023
Reported
May 17, 2023
Classified
May 6, 2023
Terminated
May 9, 2023
Quantity
4946
Location
Caledonia, MI, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

MI, OH, WI

FDA source record · F-0824-2023

Data updated September 16, 2026. View official FDA data ↗

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